HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Bromophenoxymethyl)benzoic acid → 4-Bromo-6,11-dihydrodibenz[b,e]oxepin-11-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Bromophenoxymethyl)benzoic acid | HCID 20085923 | — |
| Catalyst | Trifluoroacetic anhydride | HCID 9845 | — |
| Product | 4-Bromo-6,11-dihydrodibenz[b,e]oxepin-11-one | HCID 15113835 | 53% |
Reaction Steps
A suspension of 2-(2-bromophenoxymethyl)benzoic acid (18.8 g, 0.06 mole) in 100 mL of trifluoracetic anhydride containing ten drops of boron trifluoride-ether complex was refluxed for four hours. The mixture was poured into ice water and then extracted with diethyl ether. Concentration of the ether solution under reduced pressure gave the pure product (9.2 g), mp 127°-130° C. pmr (CDCl3) δ: 7.28-8.19 (m, 76H, aromatic H); 6.99 (t, 1H, H2); 5.30 (s, 2H, ArCH2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05395610 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-96496f62f42c43ef862c876d2c00ba5a |
| Source note | uspto-grants-1995_03 |